HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-2-(pyridin-3-yl)-6-(trifluoromethyl)pyrimidine → HCID 22732404, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-2-(pyridin-3-yl)-6-(trifluoromethyl)pyrimidine | HCID 1485990 | — |
| Reactant | 3-(2-methylpyrimidin-4-yl)aniline | HCID 2735397 | — |
| Product | HCID 22732404 | HCID 22732404 | — |
Reaction Steps
The title compound was prepared from a mixture of 4-chloro-2-(3-pyridinyl)-6-(trifluoromethyl)pyrimidine (50 mg, 0.193 mmol) and 4-(3-aminophenyl)-2-methylpyrimidine (71 mg, 0.386 mmol) similar to Example 58. The mixture was extracted with ethyl acetate (50 ml), washed with water (1×25 ml) and with aqueous 2N HCl (1×25 ml). The acidic aqueous solution was basified with aqueous 2N NaOH to pH 10-12. The resulting precipitate was filtered, washed with water and isolated as a light tan solid (18 mg, 23%). 1H NMR (CDCl3): 9.71 (d, J=2.4 Hz, 1H), 8.77-8.72 (m, 3H), 8.38 (s, 1H), 7.89 (d, J=7.2 Hz, 1H), 7.69-7.54 (m, 4H), 7.45-7.41 (m, 1H), 6.95 (s, 1H), 2.83 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06716851B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-8bf7f8700e4b46038824bd0dba120129 |
| Source note | uspto-grants-2004_04 |